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Establishing a technique for isolation and characterization of human periodontal ligament derived mesenchymal stem cells

Mesenchymal stem cells (MSCs) are extensively used in tissue regenerative procedures. One source of MSCs is the periodontal ligament (PDL) of teeth. Isolation of MSCs from extracted teeth is reasonably simple, being less invasive and presenting fewer ethical concerns than does the harvesting of MSC’...

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Autores principales: Banavar, Spoorthi Ravi, Rawal, Swati Yeshwant, Paterson, Ian Charles, Singh, Gurbind, Davamani, Fabian, Khoo, Suan Phaik, Tan, Eng Lai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8589598/
https://www.ncbi.nlm.nih.gov/pubmed/34803321
http://dx.doi.org/10.1016/j.sdentj.2020.04.007
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author Banavar, Spoorthi Ravi
Rawal, Swati Yeshwant
Paterson, Ian Charles
Singh, Gurbind
Davamani, Fabian
Khoo, Suan Phaik
Tan, Eng Lai
author_facet Banavar, Spoorthi Ravi
Rawal, Swati Yeshwant
Paterson, Ian Charles
Singh, Gurbind
Davamani, Fabian
Khoo, Suan Phaik
Tan, Eng Lai
author_sort Banavar, Spoorthi Ravi
collection PubMed
description Mesenchymal stem cells (MSCs) are extensively used in tissue regenerative procedures. One source of MSCs is the periodontal ligament (PDL) of teeth. Isolation of MSCs from extracted teeth is reasonably simple, being less invasive and presenting fewer ethical concerns than does the harvesting of MSC’s from other sites. The objectives of this study were to isolate and characterize the PDL stem cells (PDLSC) from healthy adults’ extracted teeth and then to characterize them by comparing them with bone-marrow derived MSCs (BMMSC). METHODS: The PDL tissue was scraped from the roots of freshly extracted teeth to enzymatically digest using collagenase. The cells were sub-cultured. Flow-cytometric analysis for the MSC surface-markers CD105, CD73, CD166, CD90, CD34, CD45 and HLA-DR was performed. To confirm the phenotype, total RNA was extracted to synthesize cDNA and which was then subjected to RT-PCR. The gene-expression for Oct4A, Sox2, NANOG and GAPDH was determined by gel-electrophoresis. To assess their multilineage potential, cells were cultured with osteogenic, chondrogenic and adipogenic medium and then stained by Alizarin-red, Alcian-blue and Oil-Red-O respectively. MSCs from the bone-marrow were processed similarly to serve as controls. RESULTS: The cells isolated from extracted teeth expanded successfully. On flow-cytometric analysis, the cells were positive for CD73, CD90, CD105, CD166 and negative for CD34, CD45 and HLA-DR. The PDLSCs expressed Oct4A, Sox2, and NANOG mRNA with GAPDH expression. Cells cultured in the osteogenic, chondrogenic and adipogenic media stained positive for Alizarin-red, Alcian-blue and Oil- Red-O respectively. The surface marker expression and the trilineage differentiation characteristics were comparable to those of the BMMSCs. CONCLUSIONS: The periodontal ligament tissue of extracted teeth is a potential source of therapeutically useful MSCs. Harvesting them is not invasive and are a promising source of MSC as the PDLSCs showed characteristics similar to those of the highly regarded MSC’s derived from bone-marrow.
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spelling pubmed-85895982021-11-19 Establishing a technique for isolation and characterization of human periodontal ligament derived mesenchymal stem cells Banavar, Spoorthi Ravi Rawal, Swati Yeshwant Paterson, Ian Charles Singh, Gurbind Davamani, Fabian Khoo, Suan Phaik Tan, Eng Lai Saudi Dent J Original Article Mesenchymal stem cells (MSCs) are extensively used in tissue regenerative procedures. One source of MSCs is the periodontal ligament (PDL) of teeth. Isolation of MSCs from extracted teeth is reasonably simple, being less invasive and presenting fewer ethical concerns than does the harvesting of MSC’s from other sites. The objectives of this study were to isolate and characterize the PDL stem cells (PDLSC) from healthy adults’ extracted teeth and then to characterize them by comparing them with bone-marrow derived MSCs (BMMSC). METHODS: The PDL tissue was scraped from the roots of freshly extracted teeth to enzymatically digest using collagenase. The cells were sub-cultured. Flow-cytometric analysis for the MSC surface-markers CD105, CD73, CD166, CD90, CD34, CD45 and HLA-DR was performed. To confirm the phenotype, total RNA was extracted to synthesize cDNA and which was then subjected to RT-PCR. The gene-expression for Oct4A, Sox2, NANOG and GAPDH was determined by gel-electrophoresis. To assess their multilineage potential, cells were cultured with osteogenic, chondrogenic and adipogenic medium and then stained by Alizarin-red, Alcian-blue and Oil-Red-O respectively. MSCs from the bone-marrow were processed similarly to serve as controls. RESULTS: The cells isolated from extracted teeth expanded successfully. On flow-cytometric analysis, the cells were positive for CD73, CD90, CD105, CD166 and negative for CD34, CD45 and HLA-DR. The PDLSCs expressed Oct4A, Sox2, and NANOG mRNA with GAPDH expression. Cells cultured in the osteogenic, chondrogenic and adipogenic media stained positive for Alizarin-red, Alcian-blue and Oil- Red-O respectively. The surface marker expression and the trilineage differentiation characteristics were comparable to those of the BMMSCs. CONCLUSIONS: The periodontal ligament tissue of extracted teeth is a potential source of therapeutically useful MSCs. Harvesting them is not invasive and are a promising source of MSC as the PDLSCs showed characteristics similar to those of the highly regarded MSC’s derived from bone-marrow. Elsevier 2021-11 2020-04-19 /pmc/articles/PMC8589598/ /pubmed/34803321 http://dx.doi.org/10.1016/j.sdentj.2020.04.007 Text en © 2020 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Banavar, Spoorthi Ravi
Rawal, Swati Yeshwant
Paterson, Ian Charles
Singh, Gurbind
Davamani, Fabian
Khoo, Suan Phaik
Tan, Eng Lai
Establishing a technique for isolation and characterization of human periodontal ligament derived mesenchymal stem cells
title Establishing a technique for isolation and characterization of human periodontal ligament derived mesenchymal stem cells
title_full Establishing a technique for isolation and characterization of human periodontal ligament derived mesenchymal stem cells
title_fullStr Establishing a technique for isolation and characterization of human periodontal ligament derived mesenchymal stem cells
title_full_unstemmed Establishing a technique for isolation and characterization of human periodontal ligament derived mesenchymal stem cells
title_short Establishing a technique for isolation and characterization of human periodontal ligament derived mesenchymal stem cells
title_sort establishing a technique for isolation and characterization of human periodontal ligament derived mesenchymal stem cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8589598/
https://www.ncbi.nlm.nih.gov/pubmed/34803321
http://dx.doi.org/10.1016/j.sdentj.2020.04.007
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